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N,2-diphenylquinazolin-4-amine

更新时间:2026-06-30 12:06:10

N,2-diphenylquinazolin-4-amine结构式
N,2-diphenylquinazolin-4-amine结构式
品牌特惠专场
常用名 N,2-diphenylquinazolin-4-amine 英文名 N,2-diphenylquinazolin-4-amine
CAS号 40288-70-8 分子量 297.35300
密度 N/A 沸点 N/A
分子式 C20H15N3 熔点 N/A
MSDS N/A 闪点 N/A

 N,2-diphenylquinazolin-4-amine名称

英文名 N,2-diphenylquinazolin-4-amine
英文别名 更多

 N,2-diphenylquinazolin-4-amine物理化学性质

分子式 C20H15N3
分子量 297.35300
精确质量 297.12700
PSA 41.04000
LogP 4.46230
InChIKey CMVDRFFMSYMSRT-UHFFFAOYSA-N
SMILES c1ccc(Nc2nc(-c3ccccc3)nc3ccccc23)cc1

 N,2-diphenylquinazolin-4-amine合成线路

 N,2-diphenylquinazolin-4-amine靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Luminescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of ADP-glo R...
来源:Broad Institute
靶标:N/A
External Id:2046-03_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
实验名称:Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Syn...
来源:Broad Institute
靶标:glycogen synthase kinase 3 beta isoform 1 [Homo sapiens]
External Id:2046-02_INHIBITORS_DOSE-TITRATION_MLPCN-CHERRYPICK
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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 N,2-diphenylquinazolin-4-amine英文别名

2-phenyl-4-(N-phenylamino)quinazoline
N,2-diphenyl-4-quinazolinamine
2-phenyl-4-anilinoquinazoline
Phenyl-(2-phenyl-quinazolin-4-yl)-amine
2-phenyl-4-(phenylamino)quinazoline
4-anilino-2-phenylquinazoline
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